Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:141551342-141551423 | Rare:23; Clinvar:4; Clinvar (benign):2 | ||||
chr7:141738021-141738464 | Common:4; Rare:134 | ||||
chr7:143288277-143288449 | Common:1; Rare:68 | ||||
chr7:143380954-143381293 | Common:1; Rare:107 | ||||
chr7:143882817-143882995 | Rare:48 | ||||
chr7:143902099-143902304 | Common:6; Rare:65 | ||||
chr7:149090663-149090907 | Rare:65 | ||||
chr7:149126278-149126399 | Common:5; Rare:41 | ||||
chr7:149719235-149719352 | Rare:20 | ||||
chr7:149873823-149873999 | Common:2; Rare:69 | ||||
chr7:150379070-150379347 | Common:1; Rare:98 | ||||
chr7:150800444-150800809 | Common:4; Rare:94 | ||||
chr7:151028195-151028464 | Rare:93 | ||||
chr7:151227158-151227425 | Common:1; Rare:73 | ||||
chr7:152025583-152025775 | Rare:78 |